ChemicalBook--->CAS DataBase List--->9011-93-2

9011-93-2

9011-93-2 Structure

9011-93-2 Structure
IdentificationBack Directory
[Name]

LYSOSTAPHIN
[CAS]

9011-93-2
[Synonyms]

Ambicin L
LYSOSTAPHIN
EC 3.4.24.75
E.C. 3.4.24.75
Lysostaphin from
LYSOSTAPHIN USP/EP/BP
glycyl-glycine endopeptidase
LYSOSTAPHIN AFFINITY PURIFIED
LYSOSTAPHIN ASEPTICALLY FILLED
lysostaphin from staphylococcus simulans
LYSOSTAPHIN ASEPTICALLY FILLED, BR,1200u/mg
Lysostaphin from Staphylococcus staphylolyticus
lysostaphin from staphylococcus staphy-lolyticus
Native Staphylococcus staphylolyticus Lysostaphin
LYSOSTAPHIN, STAPHYLOCOCCUS SIMULANS,*RE COMBINANT
Lysostaphin from Staphylococcus simulans, Recombinant
LYSOSTAPHIN FROM STAPHYLOCOCCUS STAPHY-L OLYTICUS, ~1 U/MG
[EINECS(EC#)]

812-596-7
[MDL Number]

MFCD00131556
Chemical PropertiesBack Directory
[storage temp. ]

-20°C
[form ]

powder
[color ]

slightly brown
[biological source]

microbial (Staphylococcus staphylotyticus)
[Water Solubility ]

water: 2.00-2.10mg/mL, clear to slightly hazy, colorless to light yellow
[Merck ]

13,5659
[Specific Activity]

≥500units/mg protein
[Major Application]

diagnostic assay manufacturing
Safety DataBack Directory
[Symbol(GHS) ]


GHS08
[Signal word ]

Danger
[Hazard statements ]

H334
[Precautionary statements ]

P261-P284-P501
[Safety Statements ]

22-24/25
[WGK Germany ]

3
[RTECS ]

OL5985000
[F ]

10-21
[HS Code ]

3507909090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Resp. Sens. 1
[Toxicity]

LD50 (7-day) in mice, rats (mg/kg): 820, 530 i.v. (Zygmunt)
Hazard InformationBack Directory
[Uses]

Lysostaphin from Staphylococcus simulans has been used in a study to assess molecular cloning, sequencing, and expression of lytM, a unique autolytic gene of Staphylococcus aureus. It has also been used in a study to investigate the sequence analysis of a Staphylococcus aureus gene encoding a peptidoglycan hydrolase activity.
[General Description]

Chemical structure: peptide
[Biochem/physiol Actions]

Lysostaphin is a zinc endopeptidase with a molecular weight of approximately 25 kDa. Because lysostaphin cleaves the polyglycine cross-links in the peptidoglycan layer of the cell wall of Staphylococcus species it has been found useful for cell lysis and also as a potential anti-microbial therapeutic. pH Optimum for activity: ~7.5
[in vivo]

Lysostaphin (5 mg/kg, intravenous injection, once daily for 3 consecutive days) effectively clears systemic Staphylococcus aureus (MSSA) infections in CF-1 mice[2]. Lysostaphin (50 mg/kg, intravenous injection, single dose) effectively clears Staphylococcus aureus (MSSA and MRSA) infections from the kidneys, spleen, and liver, but is not superior to repeated lower doses[2]. Lysostaphin (1 mg/kg, intravenous injection, once daily for 3 consecutive days) combined with Oxacillin (HY-B0925A) achieves the same antibacterial effect with a lower concentration of Lysostaphin. When combined with Vancomycin, low-dose Lysostaphin (1 mg/kg) similarly shows enhanced efficacy against MRSA[2].

Animal Model:Systemic infection model in CF-1 mice induced by methicillin-susceptible Staphylococcus aureus (MSSA) and methicillin-resistant Staphylococcus aureus (MRSA)[2]
Dosage:1, 5, 25, 50 mg/kg
Administration:Intravenous injection (i.v.), single high-dose administration: 25 mg/kg or 50 mg/kg intravenous injection, single dose; Once daily administration: 1 or 5 mg/kg, once daily for 3 days.
Result:Cleared MSSA from the blood and organs of mice (5 mg/kg for 3 days). Cleared MSSA and MRSA from the kidneys, spleen, and liver (A higher single dose of 50 mg/kg). Improved effectiveness and allowed reduction of the lysostaphin dose to 1 mg/kg for MRSA infections (Combined with Oxacillin (HY-B0925A) or Vancomycin (HY-B0671)).
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